Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4081134
MEG3
0.790 0.160 14 100855451 non coding transcript exon variant G/A snv 0.29 7
rs745805222
IGF1
0.790 0.120 12 102475722 synonymous variant C/T snv 1.2E-05 4.9E-05 7
rs10895322
MMP20
0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 4
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs41274458
KIF1B
0.851 0.080 1 10303606 missense variant G/T snv 1.8E-02 1.9E-02 4
rs758576072
RIMS2
0.851 0.160 8 104244917 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs2302616
ODC1-DT ; ODC1 ; SNORA80B
0.882 0.080 2 10448065 intron variant C/A snv 0.26 3
rs143864187
CASP4
0.882 0.080 11 104949666 missense variant C/A snv 3
rs17065417
LIN28B
0.882 0.080 6 104958399 intron variant A/C snv 0.10 3
rs221634
LIN28B
0.851 0.080 6 105080213 3 prime UTR variant T/A snv 0.52 4
rs4884357
TARDBP
0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 6
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs148634289
SDHD
0.827 0.200 11 112088925 synonymous variant C/T snv 1.6E-05 2.1E-05 6
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs2153977
MAGI3
0.807 0.240 1 113537449 intron variant C/T snv 0.28 6
rs2273267
NRAS ; CSDE1
0.882 0.080 1 114716848 upstream gene variant A/C;T snv 4
rs765771575
MET
0.882 0.080 7 116782017 missense variant T/C;G snv 4.0E-06; 4.0E-06 3
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs201668878
UBE4A
0.882 0.080 11 118373576 missense variant T/C snv 1.7E-04 1.0E-04 4
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13